Jiawang Yang , Feng Liang , Fenglin Zhang , Hailong Zhao , Qihai Gong , Ning Gao
{"title":"m6A 修饰与非编码 RNA 相互调控的最新进展及其在急性髓性白血病中的治疗应用。","authors":"Jiawang Yang , Feng Liang , Fenglin Zhang , Hailong Zhao , Qihai Gong , Ning Gao","doi":"10.1016/j.pharmthera.2024.108671","DOIUrl":null,"url":null,"abstract":"<div><p>N<sup>6</sup>-methyladenosine (m<sup>6</sup>A) is one of the most common modifications of RNA in eukaryotic cells and is involved in mRNA metabolism, including stability, translation, maturation, splicing, and export. m<sup>6</sup>A also participates in the modification of multiple types of non-coding RNAs, such as microRNAs, long non-coding RNAs, and circular RNAs, thereby affecting their metabolism and functions. Increasing evidence has revealed that m<sup>6</sup>A regulators, such as writers, erasers, and readers, perform m<sup>6</sup>A-dependent modification of ncRNAs, thus affecting cancer progression. Moreover, ncRNAs modulate m<sup>6</sup>A regulators to affect cancer development and progression. In this review, we summarize recent advances in understanding m<sup>6</sup>A modification and ncRNAs and provide insights into the interaction between m<sup>6</sup>A modification and ncRNAs in cancer. We also discuss the potential clinical applications of the mechanisms underlying the interplay between m<sup>6</sup>A modifications and ncRNAs in acute myeloid leukemia (AML). Therefore, clarifying the mutual regulation between m<sup>6</sup>A modifications and ncRNAs is of great significance to identify novel therapeutic targets for AML and has great clinical application prospects.</p></div>","PeriodicalId":402,"journal":{"name":"Pharmacology & Therapeutics","volume":"259 ","pages":"Article 108671"},"PeriodicalIF":12.0000,"publicationDate":"2024-06-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"Recent advances in the reciprocal regulation of m6A modification with non-coding RNAs and its therapeutic application in acute myeloid leukemia\",\"authors\":\"Jiawang Yang , Feng Liang , Fenglin Zhang , Hailong Zhao , Qihai Gong , Ning Gao\",\"doi\":\"10.1016/j.pharmthera.2024.108671\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<div><p>N<sup>6</sup>-methyladenosine (m<sup>6</sup>A) is one of the most common modifications of RNA in eukaryotic cells and is involved in mRNA metabolism, including stability, translation, maturation, splicing, and export. m<sup>6</sup>A also participates in the modification of multiple types of non-coding RNAs, such as microRNAs, long non-coding RNAs, and circular RNAs, thereby affecting their metabolism and functions. Increasing evidence has revealed that m<sup>6</sup>A regulators, such as writers, erasers, and readers, perform m<sup>6</sup>A-dependent modification of ncRNAs, thus affecting cancer progression. Moreover, ncRNAs modulate m<sup>6</sup>A regulators to affect cancer development and progression. In this review, we summarize recent advances in understanding m<sup>6</sup>A modification and ncRNAs and provide insights into the interaction between m<sup>6</sup>A modification and ncRNAs in cancer. We also discuss the potential clinical applications of the mechanisms underlying the interplay between m<sup>6</sup>A modifications and ncRNAs in acute myeloid leukemia (AML). Therefore, clarifying the mutual regulation between m<sup>6</sup>A modifications and ncRNAs is of great significance to identify novel therapeutic targets for AML and has great clinical application prospects.</p></div>\",\"PeriodicalId\":402,\"journal\":{\"name\":\"Pharmacology & Therapeutics\",\"volume\":\"259 \",\"pages\":\"Article 108671\"},\"PeriodicalIF\":12.0000,\"publicationDate\":\"2024-06-01\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Pharmacology & Therapeutics\",\"FirstCategoryId\":\"3\",\"ListUrlMain\":\"https://www.sciencedirect.com/science/article/pii/S0163725824000913\",\"RegionNum\":1,\"RegionCategory\":\"医学\",\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"Q1\",\"JCRName\":\"PHARMACOLOGY & PHARMACY\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Pharmacology & Therapeutics","FirstCategoryId":"3","ListUrlMain":"https://www.sciencedirect.com/science/article/pii/S0163725824000913","RegionNum":1,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q1","JCRName":"PHARMACOLOGY & PHARMACY","Score":null,"Total":0}
Recent advances in the reciprocal regulation of m6A modification with non-coding RNAs and its therapeutic application in acute myeloid leukemia
N6-methyladenosine (m6A) is one of the most common modifications of RNA in eukaryotic cells and is involved in mRNA metabolism, including stability, translation, maturation, splicing, and export. m6A also participates in the modification of multiple types of non-coding RNAs, such as microRNAs, long non-coding RNAs, and circular RNAs, thereby affecting their metabolism and functions. Increasing evidence has revealed that m6A regulators, such as writers, erasers, and readers, perform m6A-dependent modification of ncRNAs, thus affecting cancer progression. Moreover, ncRNAs modulate m6A regulators to affect cancer development and progression. In this review, we summarize recent advances in understanding m6A modification and ncRNAs and provide insights into the interaction between m6A modification and ncRNAs in cancer. We also discuss the potential clinical applications of the mechanisms underlying the interplay between m6A modifications and ncRNAs in acute myeloid leukemia (AML). Therefore, clarifying the mutual regulation between m6A modifications and ncRNAs is of great significance to identify novel therapeutic targets for AML and has great clinical application prospects.
期刊介绍:
Pharmacology & Therapeutics, in its 20th year, delivers lucid, critical, and authoritative reviews on current pharmacological topics.Articles, commissioned by the editor, follow specific author instructions.This journal maintains its scientific excellence and ranks among the top 10 most cited journals in pharmacology.